A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532164



Internal ID20905525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36793725..37314426hg38UCSC Ensembl
chr19:37284627..37805328hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38520702
hg19520702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197822
Samples
Known GenesLOC284412, ZNF345, ZNF383, ZNF420, ZNF568, ZNF585A, ZNF585B, ZNF790, ZNF790-AS1, ZNF829
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532164
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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